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Clinical Writer I

Richardson, TX, us💼 Full-time🗓 2026-07-22 → 2026-09-26

Core

Drafts and reviews clinical study protocols and reports for cosmetics and other claims, adhering to ICH and GCP guidelines.

Role type

Entry-level clinical writer (technical writing)

Builds

Clinical study protocols and clinical study reports

Domain

Life sciences / Cosmetics / Regulatory compliance

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Technical writing, editing, research, document consistency, attention to detail, organizational ability

Preferred skills

None stated

Technologies

Microsoft Word, Microsoft Excel

Responsibilities

Draft protocols and reports using templates and guidelines; coordinate internal and external protocol reviews; draft clinical study reports based on data and protocol; maintain internal databases of templates and specifications; assist in drafting SOPs and Work Instructions.

Seniority

Junior, individual contributor

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